Variant report

Variant	rs35988516
Chromosome Location	chr4:74389980-74389981
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 89 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10016403	0.92[ASN][1000 genomes]
rs10028196	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10028276	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10212657	0.94[ASN][1000 genomes]
rs10213305	0.94[ASN][1000 genomes]
rs10518115	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10805065	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10938077	0.96[ASN][1000 genomes]
rs10938078	0.96[ASN][1000 genomes]
rs10938079	0.96[ASN][1000 genomes]
rs10938085	0.89[EUR][1000 genomes]
rs10938086	0.89[EUR][1000 genomes]
rs1158101	0.86[ASN][1000 genomes]
rs1159624	0.87[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs11728915	0.83[ASN][1000 genomes]
rs11733262	0.93[ASN][1000 genomes]
rs11935001	0.94[ASN][1000 genomes]
rs11939341	0.92[ASN][1000 genomes]
rs11943798	0.90[ASN][1000 genomes]
rs1247670	0.86[EUR][1000 genomes]
rs1247671	0.81[EUR][1000 genomes]
rs12504448	0.96[ASN][1000 genomes]
rs12508661	0.85[EUR][1000 genomes]
rs12508974	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12510629	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13103378	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13107306	0.83[ASN][1000 genomes]
rs13120998	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13124940	0.93[ASN][1000 genomes]
rs13133747	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13150405	0.95[ASN][1000 genomes]
rs1358592	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.90[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1528924	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1569204	0.87[EUR][1000 genomes]
rs1590115	0.98[ASN][1000 genomes]
rs1590116	0.98[ASN][1000 genomes]
rs16849461	0.81[ASN][1000 genomes]
rs16849484	0.83[ASN][1000 genomes]
rs16849508	0.86[ASN][1000 genomes]
rs17192413	0.85[EUR][1000 genomes]
rs17805623	0.84[EUR][1000 genomes]
rs1894293	0.93[ASN][1000 genomes]
rs1919469	0.90[ASN][1000 genomes]
rs1919479	0.95[ASN][1000 genomes]
rs1997332	0.96[ASN][1000 genomes]
rs1997333	0.96[ASN][1000 genomes]
rs2040354	0.93[ASN][1000 genomes]
rs2071097	0.96[ASN][1000 genomes]
rs2071098	0.83[ASN][1000 genomes]
rs2141465	0.96[ASN][1000 genomes]
rs2141470	0.96[ASN][1000 genomes]
rs2178290	0.96[ASN][1000 genomes]
rs2178292	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2204736	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs28838047	0.81[ASN][1000 genomes]
rs34123018	0.86[EUR][1000 genomes]
rs34238679	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs34468776	0.94[ASN][1000 genomes]
rs35233345	0.94[ASN][1000 genomes]
rs3756073	0.82[EUR][1000 genomes]
rs3765639	0.82[ASN][1000 genomes]
rs4235119	0.96[ASN][1000 genomes]
rs4267703	0.96[ASN][1000 genomes]
rs4267704	0.96[ASN][1000 genomes]
rs4267705	0.96[ASN][1000 genomes]
rs4438732	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4574378	0.90[ASN][1000 genomes]
rs4618279	0.98[ASN][1000 genomes]
rs4631010	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4694170	0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4694173	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56011127	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56384466	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6446937	0.96[ASN][1000 genomes]
rs6446938	0.96[ASN][1000 genomes]
rs6446939	0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6446941	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6838329	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6852149	0.96[ASN][1000 genomes]
rs6852772	0.83[ASN][1000 genomes]
rs72647083	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs72649103	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7676460	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7687216	0.82[EUR][1000 genomes]
rs9990707	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3430875	chr4:74243646-74420354	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv1001725	chr4:74354050-74860924	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv530126	chr4:74376622-74843892	Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv3364178	chr4:74383966-74400177	Enhancers Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:74374600-74399000	Weak transcription	Fetal Intestine Large	intestine
2	chr4:74382000-74394200	Strong transcription	Liver	Liver
3	chr4:74386200-74390400	Strong transcription	Fetal Intestine Small	intestine
4	chr4:74387000-74390400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr4:74388600-74392000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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